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PRKD2 wt Allele

Known as: HSPC187, PKD2, DKFZP586E0820 
Human PRKD2 wild-type allele is located in the vicinity of 19q13.3 and is approximately 43 kb in length. This allele, which encodes serine/threonine… Expand
National Institutes of Health

Papers overview

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Review
2018
Review
2018
To the Editor: Advances in antenatal ultrasonography have substantially improved the counseling of pregnant women. 4 With this… Expand
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2015
2015
The development of diabetic cardiomyopathy is a key contributor to heart failure and mortality in obesity and type 2 diabetes… Expand
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2015
2015
The integrin α6β4, a major component of hemidesmosomes (HDs), stabilizes keratinocyte cell adhesion to the epidermal basement… Expand
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2013
2013
Abstract Context: G-protein coupled receptor (GPCR) signaling in skeletal muscle is incompletely understood; in particular, the… Expand
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2011
2011
Protein kinase D (PKD) is a subfamily of serine/threonine specific family of kinases, comprised of PKD1, PKD2 and PKD3 (PKC… Expand
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Highly Cited
2008
Highly Cited
2008
It is widely recognized that Hsp27 is a downstream substrate of the p38 MAPK cascade whereas the role of PKD family members in… Expand
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2007
2007
Angiotensin II (AII) has been reported to induce leukocyte adhesion to endothelium through up-regulation of P-selectin surface… Expand
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2006
2006
Autosomal dominant polycystic kidney disease (ADPKD) is genetically heterogeneous and is caused by mutations in the PKD1 or PKD2… Expand
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Highly Cited
2005
Highly Cited
2005
ABSTRACT PKD2, or polycystin 2, the product of the gene mutated in type 2 autosomal dominant polycystic kidney disease, belongs… Expand
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1997
1997
At least 2 genes, detectable by DNA methods, encode autosomal dominant polycystic kidney disease (ADPKD), which remains the most… Expand
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